Clinical Impact of Continued Crizotinib Administration after Isolated Central Nervous System Progression in Patients with Lung Cancer Positive for ALK Rearrangement

被引:77
作者
Takeda, Masayuki [1 ]
Okamoto, Isamu [1 ]
Nakagawa, Kazuhiko [1 ]
机构
[1] Kinki Univ, Fac Med, Dept Med Oncol, Osaka 5898511, Japan
关键词
Non-small-cell lung cancer; Crizotinib; Central nervous system; Metastasis; LEPTOMENINGEAL METASTASES; RESISTANCE; ERLOTINIB; CSF;
D O I
10.1097/JTO.0b013e31828c28e7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Although crizotinib manifests marked antitumor activity in individuals with non-small-cell lung cancer positive for ALK abnormalities, all treated patients ultimately develop resistance to this drug. The central nervous system (CNS) is a frequent site of disease progression in such patients, with palliative radiotherapy usually being administered for the CNS metastasis. However, subsequent chemotherapy has not been optimized in these patients. Methods: We retrospectively evaluated the continuation of crizotinib treatment after radiotherapy for isolated CNS progression in ALK-rearrangement-positive non-small-cell lung cancer patients. Results: Among 21 ALK-rearrangement-positive patients treated with crizotinib, seven individuals resumed daily crizotinib administration after the completion of radiotherapy for isolated CNS failure. All these patients continued to receive crizotinib for at least 4 months after radiotherapy without disease progression. One patient experienced a recurrent isolated CNS failure during the second period of crizotinib administration but subsequently resumed crizotinib treatment again for at least 8.5 months after another application of radiotherapy. Conclusions: Development of isolated CNS metastasis is emerging as a clinical concern for patients treated with crizotinib. Our data suggest that continued administration of crizotinib after radiotherapy for isolated CNS progression is a potential treatment option for such patients.
引用
收藏
页码:654 / 657
页数:4
相关论文
共 13 条
  • [1] Activity and safety of crizotinib in patients with ALK-positive non-small-cell lung cancer: updated results from a phase 1 study
    Camidge, D. Ross
    Bang, Yung-Jue
    Kwak, Eunice L.
    Iafrate, A. John
    Varella-Garcia, Marileila
    Fox, Stephen B.
    Riely, Gregory J.
    Solomon, Benjamin
    Ou, Sai-Hong I.
    Kim, Dong-Wan
    Salgia, Ravi
    Fidias, Panagiotis
    Engelman, Jeffrey A.
    Gandhi, Leena
    Jaenne, Pasi A.
    Costa, Daniel B.
    Shapiro, Geoffrey I.
    LoRusso, Patricia
    Ruffner, Katherine
    Stephenson, Patricia
    Tang, Yiyun
    Wilner, Keith
    Clark, Jeffrey W.
    Shaw, Alice T.
    [J]. LANCET ONCOLOGY, 2012, 13 (10) : 1011 - 1019
  • [2] EML4-ALK Mutations in Lung Cancer That Confer Resistance to ALK Inhibitors
    Choi, Young Lim
    Soda, Manabu
    Yamashita, Yoshihiro
    Ueno, Toshihide
    Takashima, Junpei
    Nakajima, Takahiro
    Yatabe, Yasushi
    Takeuchi, Kengo
    Hamada, Toru
    Haruta, Hidenori
    Ishikawa, Yuichi
    Kimura, Hideki
    Mitsudomi, Tetsuya
    Tanio, Yoshiro
    Mano, Hiroyuki
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (18) : 1734 - 1739
  • [3] High dose weekly erlotinib achieves therapeutic concentrations in CSF and is effective in leptomeningeal metastases from epidermal growth factor receptor mutant lung cancer
    Clarke, Jennifer L.
    Pao, William
    Wu, Nian
    Miller, Vincent A.
    Lassman, Andrew B.
    [J]. JOURNAL OF NEURO-ONCOLOGY, 2010, 99 (02) : 283 - 286
  • [4] CSF Concentration of the Anaplastic Lymphoma Kinase Inhibitor Crizotinib
    Costa, Daniel B.
    Kobayashi, Susumu
    Pandya, Shuchi S.
    Yeo, Wee-Lee
    Shen, Zhongzhou
    Tan, Weiwei
    Wilner, Keith D.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (15) : E443 - E445
  • [5] The Impact of Initial Gefitinib or Erlotinib versus Chemotherapy on Central Nervous System Progression in Advanced Non-Small Cell Lung Cancer with EGFR Mutations
    Heon, Stephanie
    Yeap, Beow Y.
    Lindeman, Neal I.
    Joshi, Victoria A.
    Butaney, Mohit
    Britt, Gregory J.
    Costa, Daniel B.
    Rabin, Michael S.
    Jackman, David M.
    Johnson, Bruce E.
    [J]. CLINICAL CANCER RESEARCH, 2012, 18 (16) : 4406 - 4414
  • [6] Response and resistance in a non-small-cell lung cancer patient with an epidermal growth factor receptor mutation and leptomeningeal metastases treated with high-dose gefitinib
    Jackman, David M.
    Holmes, Alison J.
    Lindeman, Neal
    Wen, Patrick Y.
    Kesari, Santosh
    Borras, Ana M.
    Bailey, Christopher
    de Jong, Francisca
    Jaenne, Pasi A.
    Johnson, Bruce E.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (27) : 4517 - 4520
  • [7] Current management of brain metastases, with a focus on systemic options
    Langer, CJ
    Mehta, MP
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) : 6207 - 6219
  • [8] Otterson GA, 2012, P AM SOC CLIN ONC S, V30
  • [9] Continuous EGFR-TKI administration following radiotherapy for non-small cell lung cancer patients with isolated CNS failure
    Shukuya, Takehito
    Takahashi, Toshiaki
    Naito, Tateaki
    Kaira, Rieko
    Ono, Akira
    Nakamura, Yukiko
    Tsuya, Asuka
    Kenmotsu, Hirotsugu
    Murakami, Haruyasu
    Harada, Hideyuki
    Mitsuya, Koichi
    Endo, Masahiro
    Nakasu, Yoko
    Takahashi, Kazuhisa
    Yamamoto, Nobuyuki
    [J]. LUNG CANCER, 2011, 74 (03) : 457 - 461
  • [10] Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer
    Soda, Manabu
    Choi, Young Lim
    Enomoto, Munehiro
    Takada, Shuji
    Yamashita, Yoshihiro
    Ishikawa, Shunpei
    Fujiwara, Shin-ichiro
    Watanabe, Hideki
    Kurashina, Kentaro
    Hatanaka, Hisashi
    Bando, Masashi
    Ohno, Shoji
    Ishikawa, Yuichi
    Aburatani, Hiroyuki
    Niki, Toshiro
    Sohara, Yasunori
    Sugiyama, Yukihiko
    Mano, Hiroyuki
    [J]. NATURE, 2007, 448 (7153) : 561 - U3